ENST00000373296.8:c.526T>G
MANE Select
|
ENSP00000362393.3:p.Phe176Val
|
|
ENST00000373294.8:c.526T>G
|
ENSP00000362390.5:p.Phe176Val
|
|
ENST00000373296.7:c.526T>G
|
ENSP00000362393.3:p.Phe176Val
|
|
ENST00000626498.2:c.*138T>G
|
ENSP00000487527.1:n.*138T>G
|
|
ENST00000626877.1:n.405T>G
|
|
|
NM_001109878.1:c.526T>G
|
NP_001103348.1:p.Phe176Val
|
|
NM_001109879.1:c.166T>G
|
NP_001103349.1:p.Phe56Val
|
|
NM_001303475.1:c.166T>G
|
NP_001290404.1:p.Phe56Val
|
|
NM_016954.2:c.526T>G
|
NP_058650.1:p.Phe176Val
|
|
XM_005262136.2:c.529T>G
|
XP_005262193.1:p.Phe177Val
|
|
XM_006724657.2:c.529T>G
|
XP_006724720.1:p.Phe177Val
|
|
XM_011530972.1:c.166T>G
|
XP_011529274.1:p.Phe56Val
|
|
NM_001109878.2:c.526T>G
MANE Select
|
NP_001103348.1:p.Phe176Val
|
|
NM_001109879.2:c.166T>G
|
NP_001103349.1:p.Phe56Val
|
|